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Hypophosphatemic rickets, X-linked recessive

MONDO:0010358

Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene.

Also known as: CLCN5 X-linked hypophosphatemic rickets, X-linked hypophosphatemic rickets caused by mutation in CLCN5, hypophosphatemic rickets, X-linked recessive

35 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) X-linked disease (16) Human disease (14) Rickets (10) X-linked hypophosphatemic rickets (8) Bone remodeling disease (5) Skeletal system disorder (4)
Trials to join now! 17 Not yet recruiting 6 Not yet finished but already full! 4 Completed 7 Terminated 1
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